MedPath

Juglans regia pollen

Generic Name
Juglans regia pollen
Drug Type
Biotech
Unique Ingredient Identifier
ARW43087I1

Overview

Juglans regia pollen is the pollen of the Juglans regia plant. Juglans regia pollen is mainly used in allergenic testing.

Indication

No indication information available.

Associated Conditions

No associated conditions information available.

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor

No clinical trials found

No clinical trials found for this drug

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Greer Laboratories, Inc.
22840-9488
SUBCUTANEOUS, PERCUTANEOUS, INTRADERMAL
10000 [PNU] in 1 mL
6/3/2025
Nelco Laboratories, Inc.
36987-3078
INTRADERMAL, SUBCUTANEOUS
10000 [PNU] in 1 mL
12/3/2009
Nelco Laboratories, Inc.
36987-3081
INTRADERMAL, SUBCUTANEOUS
40000 [PNU] in 1 mL
12/3/2009
Nelco Laboratories, Inc.
36987-3079
INTRADERMAL, SUBCUTANEOUS
20000 [PNU] in 1 mL
12/3/2009
Antigen Laboratories, Inc.
49288-0588
SUBCUTANEOUS, INTRADERMAL
0.0056 g in 1 mL
11/19/2009
Nelco Laboratories, Inc.
36987-3080
INTRADERMAL, SUBCUTANEOUS
20000 [PNU] in 1 mL
12/3/2009
Greer Laboratories, Inc.
22840-9487
PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL
0.05 g in 1 mL
6/3/2025
Nelco Laboratories, Inc.
36987-3083
INTRADERMAL, SUBCUTANEOUS
0.05 g in 1 mL
12/3/2009
Nelco Laboratories, Inc.
36987-3077
INTRADERMAL, SUBCUTANEOUS
10000 [PNU] in 1 mL
12/3/2009
Greer Laboratories, Inc.
22840-9807
PERCUTANEOUS, SUBCUTANEOUS, INTRADERMAL
0.025 g in 1 mL
6/3/2025

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
No HSA approvals found for this drug.

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
No PPB approvals found for this drug.

TGA Drug Approvals

Approved Product
ARTG ID
Sponsor
Registration Type
Status
Registration Date
Cerebral Tonic Pills
320146
Well Herb Pty Ltd
Medicine
A
7/15/2019
New Nordic Clear Brain
331782
Medicine
A
3/20/2020
Skin-detoxing Pills (Pifubing Xueduwan)
124896
Medicine
A
1/11/2006
LYMPHOMYOSOT
440431
Medicine
A
2/9/2024
Rest&Quiet Kids Formula
421670
Medicine
A
9/12/2023

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
LYPHOSOT - TAB
02229577
Tablet - Oral
3 D
10/11/1996
R 60 LIQ
dr reckeweg canada
02038935
Liquid - Oral
6 D / ML
12/31/1993
P SHAMPOO
terra botanica products ltd.
02233357
Liquid - Topical
1 X
5/25/1998
LYPHOSOT - LIQ
02229576
Liquid - Oral
3 D / 1.1 ML
10/1/1996
LYPHOSOT - DROPS
02229573
Drops - Oral
3 D / ML
10/1/1996
JUGLANS REGIA
seroyal international inc.
02233155
Globules ,  Drops ,  Liquid ,  Pellet ,  Tablet ,  Granules - Oral
1 X
4/6/1998
HOMEOPATHIC MEDICINE (S#923) DPS 30C
total health centre
02093464
Drops - Oral
30 C / ML
12/31/1994
JUGLANS REGIA
dolisos canada inc.
02234558
Granules ,  Liquid ,  Globules - Oral
1 X
1/5/1998
ACNE RELIEF MEDICATION
general nutrition canada inc.
02248160
Tablet - Oral
6 X
11/25/2005
R 53 DPS
dr reckeweg canada
02098814
Drops - Oral
30 D / 10 ML
12/31/1994

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
No CIMA AEMPS (Spain) approvals found for this drug.

Philippines FDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

Approved Product
Company
Registration Number
Dosage Form
Strength
Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

Medicine Name
MA Holder
MA Number
Pharmaceutical Form
Active Ingredient
Authorization Date
No UK EMC drug information found for this drug.

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